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首页> 外文期刊>Journal of clinical psychopharmacology >Does atomoxetine improve executive function, inhibitory control, and hyperactivity?: Results from a placebo-controlled trial using quantitative measurement technology
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Does atomoxetine improve executive function, inhibitory control, and hyperactivity?: Results from a placebo-controlled trial using quantitative measurement technology

机译:阿莫西汀是否改善执行功能,抑制控制和活动亢进?:使用定量测量技术的安慰剂对照试验的结果

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The primary objective of this study was to evaluate the efficacy of atomoxetine (ATX) on attention-deficit/hyperactivity disorder (ADHD)-related symptoms assessed as standard variables of a computer-based continuous performance test (cb-CPT) combined with a motion-tracking (MT) device. This was a 2-arm, 8-week, randomized, double-blind, placebo-controlled study in patients with ADHD (6-12 years). Therapy with ATX started with 0.5 mg/kg per day for 1 week, followed by 7 weeks on the target dosage of 1.2 mg/kg per day. Primary outcomes were cb-CPT/MT standard scores after 8 weeks using mixed models for repeated measurements. In addition, investigator-rated ADHD Rating Scale (ADHD-RS), Weekly Ratings of Evening and Morning Behavior (WREMB), and Clinical Global Impression-Severity-ADHD (CGI-S-ADHD) scores were assessed. Of 128 patients randomized, 125 were evaluated (ATX/placebo: 63/62). Baseline characteristics were comparable in both groups (overall, 80.2% boys; mean [SD] age, 9.0 [1.79] years; comorbid Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition diagnosis, 40.0% oppositional defiant disorder/conduct disorder; prior stimulant treatment, 24.8%; ADHD-RS total score, 36.99 [11.56]). At week 8, all cb-CPT/MT q-scores were significantly reduced versus placebo (all P < 0.001) with effect sizes (ESs) of reaction time (RT) variation (ES = 0.71), mean RT (ES = 0.41), number of microevents (ES = 1.00), commission error rate (ES = 0.50), distance of movement (ES = 0.90), area of movement (ES = 1.08), omission error rate (ES = 0.70), time active (ES = 0.69), motion simplicity (ES = 0.38), and normalized variance of RT (ES = 0.50). Secondary end points also improved significantly in favor of ATX: ADHD-RS (total score ES = 1.30, P < 0.001; hyperactivity/impulsivity subscore ES = 1.37, P < 0.001; inattention subscore ES = 1.07, P < 0.001), WREMB (total score ES = 1.00, P < 0.001; morning subscore ES = 0.59, P = 0.002; evening subscore ES = 1.02, P < 0.001), CGI-S-ADHD (ES = 1.11, P < 0.001). The results of this study show that ATX for 8 weeks significantly reduced ADHD-related symptoms as measured by the cb-CPT/MT.
机译:这项研究的主要目的是评估阿莫西汀(ATX)对注意力缺陷/多动障碍(ADHD)相关症状的疗效,这些症状被评估为基于计算机的连续性能测试(cb-CPT)与运动相结合的标准变量跟踪(MT)设备。这是一项针对多动症患者(6至12岁)的2臂,8周,随机,双盲,安慰剂对照研究。 ATX的治疗开始于每天0.5 mg / kg,持续1周,然后以每天1.2 mg / kg的目标剂量治疗7周。主要结果是使用混合模型进行重复测量的8周后的cb-CPT / MT标准评分。此外,还评估了研究者评定的ADHD评定量表(ADHD-RS),每周晚上和早晨行为评定(WREMB)以及临床总体印象-严重性ADHD(CGI-S-ADHD)得分。在随机分配的128位患者中,有125位接受了评估(ATX /安慰剂:63/62)。两组的基线特征具有可比性(总体上,男孩为80.2%;平均[SD]年龄为9.0 [1.79]岁;合并症《精神障碍诊断和统计手册》,第四版诊断,对立违抗行为/品行障碍为40.0%;先前的兴奋剂治疗为24.8%; ADHD-RS总得分为36.99 [11.56])。在第8周时,与安慰剂相比,所有cb-CPT / MT q得分均显着降低(所有P <0.001),且反应时间(RT)变化的效应大小(ESs)(ES = 0.71),平均RT(ES = 0.41) ,微事件数(ES = 1.00),佣金错误率(ES = 0.50),移动距离(ES = 0.90),移动区域(ES = 1.08),遗漏错误率(ES = 0.70),激活时间(ES = 0.69),运动简单度(ES = 0.38)和RT的标准化方差(ES = 0.50)。次要终点也显着改善,支持ATX:ADHD-RS(总分ES = 1.30,P <0.001;多动/冲动分ES = 1.37,P <0.001;注意力不集中分ES = 1.07,P <0.001),WREMB(总分ES = 1.00,P <0.001;早晨分ES = 0.59,P = 0.002;晚上分ES = 1.02,P <0.001),CGI-S-ADHD(ES = 1.11,P <0.001)。这项研究的结果表明,用cb-CPT / MT测量,ATX连续8周可显着减轻ADHD相关症状。

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